PUBLIKATIONEN - vor 2008

 2007:

Hempelmann A, Cobilanschi J, Heils A, Muhle H, Stephani U, Weber Y, Lerche H, Sander T. Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy. Epilepsy Res. 2007 Apr;74(1):28-32.

2006:

Ayerdi-Izquierdo A, Stavrides G, Sellés-Martínez JJ, Larrea L, Bovo G, López de Munain A, Bisulli F, Martí-Massó JF, Michelucci R, Poza JJ, Tinuper P, Stephani U, Striano P, Striano S, Staub E, Sarafidou T, Hinzmann B, Moschonas N, Siebert R, Deloukas P, Nobile C, Pérez-Tur J. Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. Epilepsy Res. 2006 Aug;70(2-3):118-26.

Lorenz S, Taylor KP, Gehrmann A, Becker T, Muhle H, Gresch M, Tauer U, Sander T, Stephani U. Association of BRD2 polymorphisms with photoparoxysmal response. Neurosci Lett. 2006 May 29;400(1-2):135-9.

Lorenz S, Heils A, Taylor KP, Gehrmann A, Muhle H, Gresch M, Becker T, Tauer U, Stephani U, Sander T. Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity. Neurosci Lett. 2006 Apr 24;397(3):234-9.

Kearney JA, Wiste AK, Stephani U, Trudeau MM, Siegel A, Ramachandran Nair R, Elterman RD, Muhle H, Reinsdorf J, Shields WD, Meisler MH, Escayg A. Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy. Pediatr Neurol. 2006 Feb;34(2):116-20.

2005:
Ebach K, Joos H, Doose H, Stephani U, Kurlemann G, Fiedler B, Hahn A, Hauser E, Hundt K, Holthausen H, Müller U, Neubauer BA. SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures. Neuropediatrics. 2005 Jun;36(3):210-3.

Tauer U, Lorenz S, Lenzen KP, Heils A, Muhle H, Gresch M, Neubauer BA, Waltz S, Rudolf G, Mattheisen M, Strauch K, Nürnberg P, Schmitz B, Stephani U, Sander T. Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Ann Neurol. 2005 Jun;57(6):866-73.

Neubauer BA, Waltz S, Grothe M, Hahn A, Tuxhorn I, Sander T, Kurlemann G, Stephani U. Photosensitivity: genetics and clinical significance. Adv Neurol. 2005;95:217-26.